Cortexolone-17α-propionate is a topical antiandrogen under investigation for the treatment of androgen-related skin disorders. A full conformational characterization was realized, in comparison with other steroidal androgens and antiandrogens, by means of theoretical calculations at the B3LYP/6-31G(d) level supported by high-field NMR analyses. All of the studied molecules showed a good overlay; nevertheless, the different functional groups present in the skeleton of the molecules drive the individual biological profile.

Ferraboschi, P., Legnani, L., Celasco, G., Moro, L., Ragonesi, L., & Colombo, D. (2014). A full conformational characterization of antiandrogen cortexolone-17α-propionate and related compounds through theoretical calculations and nuclear magnetic resonance spectroscopy. MEDCHEMCOMM, 5(7), 904-914 [10.1039/c4md00049h].

A full conformational characterization of antiandrogen cortexolone-17α-propionate and related compounds through theoretical calculations and nuclear magnetic resonance spectroscopy

Laura Legnani;
2014

Abstract

Cortexolone-17α-propionate is a topical antiandrogen under investigation for the treatment of androgen-related skin disorders. A full conformational characterization was realized, in comparison with other steroidal androgens and antiandrogens, by means of theoretical calculations at the B3LYP/6-31G(d) level supported by high-field NMR analyses. All of the studied molecules showed a good overlay; nevertheless, the different functional groups present in the skeleton of the molecules drive the individual biological profile.
Articolo in rivista - Articolo scientifico
molecular modeling; NMR spectroscopy; Steroids;
English
904
914
11
Ferraboschi, P., Legnani, L., Celasco, G., Moro, L., Ragonesi, L., & Colombo, D. (2014). A full conformational characterization of antiandrogen cortexolone-17α-propionate and related compounds through theoretical calculations and nuclear magnetic resonance spectroscopy. MEDCHEMCOMM, 5(7), 904-914 [10.1039/c4md00049h].
Ferraboschi, P; Legnani, L; Celasco, G; Moro, L; Ragonesi, L; Colombo, D
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/352055
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